fluoxetine
Generic: fluoxetine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
fluoxetine
Generic Name
fluoxetine hydrochloride
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
fluoxetine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6065
Product ID
50090-6065_60f6e474-597b-4231-b421-e4ef1c193f47
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078619
Listing Expiration
2026-12-31
Marketing Start
2008-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906065
Hyphenated Format
50090-6065
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
fluoxetine (source: ndc)
Generic Name
fluoxetine hydrochloride (source: ndc)
Application Number
ANDA078619 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (50090-6065-0)
- 90 CAPSULE in 1 BOTTLE (50090-6065-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "60f6e474-597b-4231-b421-e4ef1c193f47", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["1226a67f-ec09-42f6-9d1b-9ddd862ea0a0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6065-0)", "package_ndc": "50090-6065-0", "marketing_start_date": "20220909"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6065-2)", "package_ndc": "50090-6065-2", "marketing_start_date": "20220909"}], "brand_name": "Fluoxetine", "product_id": "50090-6065_60f6e474-597b-4231-b421-e4ef1c193f47", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6065", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20261231"}